Job Responsibilities
Handling and troubleshooting of sterile manufacturing and filling equipment.
Managing equipment breakdown activities, root cause analysis, and CAPA implementation.
Preparation, review, and execution of equipment qualification documents and technical documentation.
Monitoring preventive maintenance activities to ensure minimum equipment downtime.
Execution and monitoring of production and engineering activities in compliance with c GMP requirements.
Preparation and review of SOPs, protocols, reports, and other GMP documentation.
Ensuring adherence to aseptic practices and cleanroom behavior standards.
Independently handling and managing shopfloor activities effectively.
Eligibility Criteria
Minimum 6 years of relevant experience in sterile pharmaceutical manufacturing facilities.
Candidates from sterile injectable pharmaceutical facilities will be preferred.
Immediate joiners or candidates serving short notice periods will be pref...